C21ORF59 FISH Probe

The C21ORF59 FISH probe is designed to hybridize to the C21orf59 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.

SKU Test Kits Buffer Dye Color Order Now
C21orf59-20-OR  (Standard Design) 20 (40 μL) 200 μL
C21orf59-20-RE 20 (40 μL) 200 μL
C21orf59-20-GO 20 (40 μL) 200 μL
C21orf59-20-GR 20 (40 μL) 200 μL
C21orf59-20-AQ 20 (40 μL) 200 μL
C21orf59-20-DIG 20 (40 μL) 200 μL
C21orf59-20-BIO 20 (40 μL) 200 μL

Gene Summary

This gene encodes a protein that plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Naturally occuring readthrough transcription occurs from this locus to the downstream t-complex 10 like (TCP10L) gene. [provided by RefSeq, Apr 2017]

Gene Details

Gene Symbol: C21orf59

Gene Name: Chromosome 21 Open Reading Frame 59

Chromosome: CHR21: 33973983-33984918

Locus: 21q22.11

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Scientific Citations

There are currently no FISH related citations for this gene.

Product Details

Product: C21ORF59 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: C21orf59-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping